Canonical Allele Identifier: CA2587922529

Gene: INSR

Linked Data

• gnomAD v4: 19-7129053-GTTCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7129058_7129061del , CM000681.2:g.7129058_7129061del	GRCh38
NC_000019.9:g.7129069_7129072del , CM000681.1:g.7129069_7129072del	GRCh37
NC_000019.8:g.7080069_7080072del	NCBI36
NG_008852.2:g.169944_169947del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2843-103_2843-100del MANE Select	ENSP00000303830.4:n.2843-103_2843-100del
ENST00000302850.9:c.2843-103_2843-100del	ENSP00000303830.4:n.2843-103_2843-100del
ENST00000341500.9:c.2807-103_2807-100del	ENSP00000342838.4:n.2807-103_2807-100del
NM_000208.2:c.2843-103_2843-100del	NP_000199.2:n.2843-103_2843-100del
NM_000208.3:c.2843-103_2843-100del	NP_000199.2:n.2843-103_2843-100del
NM_001079817.1:c.2807-103_2807-100del	NP_001073285.1:n.2807-103_2807-100del
NM_001079817.2:c.2807-103_2807-100del	NP_001073285.1:n.2807-103_2807-100del
XM_011527988.1:c.2921-106_2921-103del	XP_011526290.1:n.2921-106_2921-103del
XM_011527989.1:c.2885-106_2885-103del	XP_011526291.1:n.2885-106_2885-103del
XM_011527988.2:c.2843-106_2843-103del	XP_011526290.2:n.2843-106_2843-103del
XM_011527989.3:c.2807-106_2807-103del	XP_011526291.2:n.2807-106_2807-103del
NM_000208.4:c.2843-103_2843-100del MANE Select	NP_000199.2:n.2843-103_2843-100del
NM_001079817.3:c.2807-103_2807-100del	NP_001073285.1:n.2807-103_2807-100del